Citric Acid → HCID 19813042, 화합물

HRID 466964노트

반응식

HRID 466964 반응식
[NH:1]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[C:5](=[O:12])[NH:4][C:3](=[O:13])[CH2:2]1.[Br:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]Br.[H-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O.C(=O)([O-])O.[Na+]>CN(C)C=O.O>[Br:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][N:4]1[C:5](=[O:12])[C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[NH:1][CH2:2][C:3]1=[O:13]

참가 물질

8

반응물 5

HCID 311Citric AcidHCID 81001,5-DibromopentaneHCID 24758Sodium hydrideHCID 516892Sodium BicarbonateHCID 19024281HCID 19024281, 화합물

생성물 1

HCID 19813042HCID 19813042, 화합물수율 52.8%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

실험 절차

In 10 ml of dimethylformamide (DMF) was dissolved 100 mg of 2,3,4,5-tetrahydro-1,4-benzodiazepine-3,5-dione and the solution then ice-cooled. Then, to the resulting solution were added 0.116 ml (1.5 equivalent) of 1,5-dibromopentane and 27.3 mg (1.2 equivalent) of a 60% sodium hydride oil dispersion and the mixture was stirred for 2 hours with ice-cooling. The reaction solution was poured into ice-cooled water containing citric acid, made alkaline with sodium hydrogen carbonate, and extracted with ethyl acetate. The ethyl acetate phase was then washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The product was purified in the same manner as in Reference Example 1 to give 97.5 mg (yield: 52.8%) of the title compound.

후처리

  1. temperaturethe solution then ice-cooled
  2. temperaturecooling
  3. additionThe reaction solution was poured into ice-
  4. extractionextracted with ethyl acetate
  5. washThe ethyl acetate phase was then washed with an aqueous saturated sodium chloride solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe product was purified in the same manner as in Reference Example 1

출처 및 근거

ORD 기록
ord-69e22f3d838e418d95572570b8f4ab9f
출처 데이터셋
uspto-grants-1992_10
특허 번호
US05158947

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